PJ STATISTICS

Thorough planning and designing as well as a proper preparation of (clinical) studies with regard to statistical aspects (sample size/power calculations (using nQuery Advisor® & nTerim® as well as PASS®), statistical sections in protocols, analysis plans, randomisations with emergency envelopes if required) are essential prerequisites for a statistically sound evaluation with software in line with the industry standard (SAS®, Phoenix WinNonlin®, R) and the correct interpretation of results in a report and/or in a presentation... Due to the activities as a biostatistician in a contract research organisation the experiences cover a broad range of indication areas. Specialising in consulting clinical researchers statistically focussing on early phase studies ("first in man" to "proof of concept", "pharmacokinetic"/-dynamic studies) was a consequence of the job as Director Biostatistics Clinical Pharmacology/Early Phase from 2004 to 2010.

Primary location: Berlin